Acetic Acid

Acetic Acid

SCHEMBL9604109

CC(=O)O.O=c1cccc[nH]1.O=c1cccn[nH]1

nearest known ligand 0.52

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Acetic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
FKBP5 Q13451 1/20 0.52
HCAR2 Q8TDS4 1/20 0.34
NPC1 O15118 2/20 0.34
RAB9A P51151 2/20 0.34
ALOX15 P16050 1/20 0.34
CDK2 P24941 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
PTGS1 P23219 1/20 0.33
KMT2A Q03164 1/20 0.33
CD74 P04233 1/20 0.33
MIF P14174 1/20 0.33
NOTUM Q6P988 1/20 0.33
NAPRT Q6XQN6 1/20 0.33
CYP1A2 P05177 1/20 0.32
SCN4A P35499 1/20 0.31
ALDH1A1 P00352 2/20 0.31
HTT P42858 1/20 0.31
BCAT2 O15382 1/20 0.30

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Acetic Acid SCHEMBL4456446 0.88 HCAR2 (0.42) HCAR2NPC1RAB9AALOX15CDK2
Acetic Acid SCHEMBL5993449 0.84 FKBP5 (0.73) FKBP5RAB9ASMN1; SMN2KMT2ANOTUM
Pyridine SCHEMBL4462835 0.81 HCAR2 (0.37) HCAR2NPC1RAB9AALOX15CDK2
Bicarbonate SCHEMBL14880924 0.80 HCAR2 (0.45) HCAR2NPC1RAB9AALOX15CDK2
Carbamic Acid SCHEMBL30801127 0.79 HCAR2 (0.43) HCAR2NPC1RAB9AALOX15CDK2
Oxalic Acid SCHEMBL27558037 0.79 HCAR2 (0.43) HCAR2NPC1RAB9AALOX15CDK2
Methyl Alcohol SCHEMBL27901542 0.78
Acetone SCHEMBL27901178 0.78 FKBP5 (0.76) FKBP5L3MBTL1KMT2ANOTUMNAPRT
Benzene SCHEMBL27553953 0.78 CYP1A2 (0.40) FKBP5HCAR2NPC1RAB9AALOX15
SCHEMBL14767914 0.76 CYP1A2 (0.43) FKBP5HCAR2NPC1RAB9AALOX15

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 6 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1025855-C Process and intermediates for prepation of oxophthalazinyl acetic acids and analogs thereof PFIZER (US) 1994-09-07 CN disclosed
US-5182391-A Process and intermediates for the preparation of oxophthalazinyl acetic acids and analogs thereof PFIZER INC. (US) 1993-01-26 US disclosed
US-5171862-A Process and indazole intermediates for the preparation of oxophthalazinyl acetic acids and analogs thereof PFIZER INC. (US) 1992-12-15 US disclosed
US-5075442-A Process and intermediates for the preparation of oxophthalazinyl acetic acids and analogs thereof PFIZER INC. (US) 1991-12-24 US disclosed
EP-0397350-A1 Process and intermediates for the preparation of oxophthalazinyl acetic acids and analogs thereof PFIZER INC. (US) 1990-11-14 EP disclosed
US-4954629-A Process and intermediates for the preparation of oxophthalazinyl acetic acids and analogs thereof PFIZER INC. (US) 1990-09-04 US disclosed